GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xylF in Pseudomonas fluorescens FW300-N2E2

Align D-xylose ABC transporter, periplasmic D-xylose-binding protein (characterized)
to candidate Pf6N2E2_1455 Xylose ABC transporter, periplasmic xylose-binding protein XylF

Query= CharProtDB::CH_003787
         (330 letters)



>FitnessBrowser__pseudo6_N2E2:Pf6N2E2_1455
          Length = 333

 Score =  391 bits (1004), Expect = e-113
 Identities = 197/327 (60%), Positives = 251/327 (76%), Gaps = 1/327 (0%)

Query: 4   KNILLTLCTSLLLTNVAAHAKEVKIGMAIDDLRLERWQKDRDIFVKKAESLGAKVFVQSA 63
           K  LL    +LL   V A A   KIG +IDDLRLERW +DRD FV  AE L AKVFVQSA
Sbjct: 5   KRTLLAGALALLSLPVMADAAHPKIGFSIDDLRLERWSRDRDYFVAAAEKLDAKVFVQSA 64

Query: 64  NGNEETQMSQIENMINRGVDVLVIIPYNGQVLSNVVKEAKQEGIKVLAYDRMINDADIDF 123
           + NE+ Q+SQIEN+I+RGVDV+VI+P+N  VL+N V EAK+ GIKV++YDR+I +ADID 
Sbjct: 65  DANEQKQISQIENLISRGVDVIVIVPFNATVLTNAVAEAKKAGIKVVSYDRLILNADIDA 124

Query: 124 YISFDNEKVGELQAKALVDIVPQGNYFLMGGSPVDNNAKLFRAGQMKVLKPYVDSGKIKV 183
           YISFDNEKVGE+QA  ++   P+GNYFL+GG+P DNNAK+ R GQMKVL+P +D G IK+
Sbjct: 125 YISFDNEKVGEMQASGVLKAAPKGNYFLLGGAPTDNNAKVLREGQMKVLQPAIDKGDIKI 184

Query: 184 VGDQWVDGWLPENALKIMENALTANNNKIDAVVASNDATAGGAIQALSAQGLSGKVAISG 243
           VG QWV  W P  AL I+ENALT NNNKID +VASNDATAGGAIQAL+AQ ++GKV ISG
Sbjct: 185 VGQQWVKEWNPTEALSIVENALTRNNNKIDGIVASNDATAGGAIQALAAQKMAGKVPISG 244

Query: 244 QDADLAGIKRIAAGTQTMTVYKPITLLANTAAEIAVELGNGQEPKADTTLNNGLKDVPSR 303
           QDADLA +KR+  GTQTMTVYKP+ L+A+ AA+++V+L   ++P   +  +NG K V + 
Sbjct: 245 QDADLAAVKRVIDGTQTMTVYKPLKLIASEAAKLSVQLARNEKPTFSSQYDNGSKKVDTI 304

Query: 304 LLTPIDVNKNNIKDTVIKDGFHKESEL 330
           LLTP  + K+NI D + KDGF+ ++++
Sbjct: 305 LLTPTPLTKDNI-DLLEKDGFYTKAQI 330


Lambda     K      H
   0.314    0.132    0.366 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 352
Number of extensions: 4
Number of successful extensions: 1
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 330
Length of database: 333
Length adjustment: 28
Effective length of query: 302
Effective length of database: 305
Effective search space:    92110
Effective search space used:    92110
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory